Basic & Clinical Medicine ›› 2023, Vol. 43 ›› Issue (6): 889-897.doi: 10.16352/j.issn.1001-6325.2023.06.0889

• Original Articles • Previous Articles     Next Articles

AHR regulates the immunomodulatory function of human adipose-derived mesenchymal stem cells

WU Wenjing1, GAO Jingxi1, ZHAO Xiaoyan1, SUN Zhao2, HAN Qin1*, ZHAO Chunhua1*   

  1. 1. Center for Excellence in Tissue Engineering,Chinese Academy of Medical Sciences, Institute of Basic Medical Sciences CAMS, School of Basic Medicine PUMC, Beijing 100005;
    2. Department of Oncology, Peking Union Medical College Hospital, CAMS & PUMC,Beijing 100730, China
  • Received:2023-03-24 Revised:2023-04-19 Online:2023-06-05 Published:2023-05-31
  • Contact: *hanqinhanqin@126.com; zhaochunhua@ibms.pumc.edu.cn

Abstract: Objective To explore the effect of aryl hydrocarbon receptor(AHR) on the immunomodulatory function of human adipose derived mesenchymal stem cells (MSCs). Methods RT-qPCR and immunofluorescence staining were used to detect the expression levels of indoleamine 2,3-dioxygenase 1 (IDO1), interleukin-4-inducible gene 1 (IL4I1) and AHR in MSCs before and after inflammatory cytokine stimulation; siCtrl, siIDO1, siIL4I1 and siAHR were transfected into MSCs and blocked the AHR signaling pathway; conditioned medium from MSCs was co-incubated with macrophages, RT-qPCR and ELISA were performed to detect the level of IL-6, IL-1β, TNF-α. Results MSCs without cytokine stimulation highly expressed AHR and hardly expressed IDO1 and IL4I1 proteins; IDO1, IL4I1 and AHR were up-regulated after different cytokine stimulation(P<0.05), the expression of IDO1 and IL4I1 was most significantly up-regulated after stimulation by IFN-γ(P<0.001), AHR entering the nucleus was increased; down-regulation of AHR expression could inhibit the immunomodulatory effect of MSCs(P<0.05). Conclusions AHR regulates the immune function of MSCs, downregulates expression of AHR could inhibit the immunomodulatory effects of MSCs.

Key words: aryl hydrocarbon receptor(AHR), mesenchymal stem cells, immunomodulatory effects

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